A5034321256- Child Nutrition and Water Access
- Iron Metabolism and Disorders
- Hemoglobinopathies and Related Disorders
- Child Nutrition and Feeding Issues
- Nutrition and Health in Aging
- Folate and B Vitamins Research
- Erythropoietin and Anemia Treatment
- Pancreatic function and diabetes
- Mycobacterium research and diagnosis
- Metabolism and Genetic Disorders
- Childhood Cancer Survivors' Quality of Life
- Immunodeficiency and Autoimmune Disorders
- Neonatal Health and Biochemistry
- Diabetes and associated disorders
- Diet and metabolism studies
- Clinical Nutrition and Gastroenterology
- Tuberculosis Research and Epidemiology
- Diabetes Management and Research
- Health and Lifestyle Studies
- Trace Elements in Health
Complejo Hospitalario Torrecárdenas
2007-2021
Abstract Treatment with nitisinone (NTBC) has brought about a drastic improvement in the treatment and prognosis of hereditary tyrosinemia type I (HT1). We conducted retrospective observational multicentric study Spanish HT1 patients treated NTBC to assess clinical biochemical long-term evolution. evaluated 52 patients, 7 adults 45 children, considering: age at diagnosis, diagnosis by symptoms, or newborn screening (NBS); phenotype (acute/subacute/chronic), mutational analysis; symptoms...
The aim of the present study was to assess reproducibility and inter-rater reliability 2 nutritional screening tools (NST): Screening Tool for Risk on Nutritional Status Growth (STRONGkids) Assessment Malnutrition in Paediatrics (STAMP).Prospective observational multicentre study. Patients ages 1 month or older admitted paediatric surgical wards were tested within 24 hours admission by independent observers: experts specialized nutrition (physicians dieticians) clinical staff nonexpert...
Reticulocyte hemoglobin content (CHr) is considered an indicator of functional iron deficiency, but understudied in children. The goals this study are to determine the reference intervals for CHr healthy children, and their relation with parameters, erythropoiesis, individual conditions. A total 902 children without aged 1 11 years were analyzed a cross-sectional study. Besides physical examination subjects questionnaire completed by parents, complete blood count, serum transferrin receptor,...
ABSTARCT The aims of this study were to determine appropriate reference ranges for serum transferrin receptor (sTfR) and sTfR/log ferritin (sTfR-F index) in healthy children their relationship with iron parameters, erythropoiesis, other conditions presented by the subject. A total 902 normal status, aged 1-11 years, included a cross-sectional study. physical examination was conducted z-score body mass index (zBMI) obtained. Complete blood count, biomarkers, erythropoietin, C-reactive...
Deficiency in the interleukin12/INFgamma pathway is a genetic condition that predisposes to some infections, including nontuberculous mycobacteria infection and extraintestinal salmonellosis. We report 2 cases sisters who were diagnosed with defect caused by new mutation Interleukin-12 receptor β1 chain (IL12Rβ1) leading different clinical presentations responses therapy.